cysteine and Thrombopenia

cysteine has been researched along with Thrombopenia in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Auton, M; Brehm, MA; Frontroth, JP; Machha, VR; Mayne, L; Obser, T; Schneppenheim, R; Tischer, A; Walter Englander, S1
Del Vecchio Blanco, C; Falciani, M; Federico, A; Filippelli, A; Floreani, A; Loguercio, C; Naccarato, R; Rossi, F; Tiso, A; Tuccillo, C1
Kalb, R; Kiefel, V; Kroll, H; Mueller-Eckhardt, C; Newman, PJ; Santoso, S; Walka, M1
Alexander, WS; Dunn, AR; Maurer, AB; Metcalf, D; Nicola, NA; Roberts, AW1
Carl, B; Kiefel, V; Kroll, H; Rahman, A; Richter, IG; Sachs, UJ; Santoso, S1
Fressinaud, E; Mazurier, C; Meyer, D1

Reviews

2 review(s) available for cysteine and Thrombopenia

ArticleYear
Studies of the c-Mpl thrombopoietin receptor through gene disruption and activation.
    Stem cells (Dayton, Ohio), 1996, Volume: 14 Suppl 1

    Topics: Animals; Bone Marrow Cells; Cysteine; Dimerization; DNA, Complementary; Gene Expression Regulation; Hematopoietic Stem Cells; Homozygote; Ligands; Liver; Megakaryocytes; Mice; Mice, Knockout; Models, Genetic; Mutagenesis; Neoplasm Proteins; Phenotype; Phosphorylation; Protein Structure, Tertiary; Proto-Oncogene Proteins; Receptors, Cytokine; Receptors, Thrombopoietin; Recombination, Genetic; Signal Transduction; Thrombocytopenia; Thrombopoietin

1996
Molecular genetics of type 2 von Willebrand disease.
    International journal of hematology, 2002, Volume: 75, Issue:1

    Topics: Adult; Amino Acid Substitution; Biopolymers; Blood Platelets; Chromosomes, Human, Pair 12; Collagen; Cysteine; DNA Mutational Analysis; Exocytosis; Exons; Female; Genes, Dominant; Genes, Recessive; Hemophilia A; Hemorrhagic Disorders; Humans; Infant, Newborn; Male; Molecular Weight; Mutation, Missense; Platelet Adhesiveness; Platelet Glycoprotein GPIb-IX Complex; Pregnancy; Pregnancy Complications, Hematologic; Protein Binding; Protein Precursors; Protein Processing, Post-Translational; Protein Structure, Tertiary; Structure-Activity Relationship; Thrombocytopenia; von Willebrand Diseases; von Willebrand Factor

2002

Other Studies

4 other study(ies) available for cysteine and Thrombopenia

ArticleYear
Enhanced Local Disorder in a Clinically Elusive von Willebrand Factor Provokes High-Affinity Platelet Clumping.
    Journal of molecular biology, 2017, 07-07, Volume: 429, Issue:14

    Topics: Amino Acid Substitution; Child; Cysteine; Deamino Arginine Vasopressin; Disulfides; Female; Humans; Mass Spectrometry; Mutant Proteins; Mutation, Missense; Platelet Aggregation; Platelet Glycoprotein GPIb-IX Complex; Plethysmography, Impedance; Surface Plasmon Resonance; Thrombocytopenia; von Willebrand Factor

2017
Platelet aggregation is affected by nitrosothiols in patients with chronic hepatitis: in vivo and in vitro studies.
    World journal of gastroenterology, 2007, Jul-21, Volume: 13, Issue:27

    Topics: Adult; Aged; Aged, 80 and over; Aldehydes; Biomarkers; Blood Platelets; Case-Control Studies; Cysteine; Female; Glutathione; Hepatitis C, Chronic; Humans; Interleukin-6; Male; Malondialdehyde; Middle Aged; Nitric Oxide; Nitrites; Platelet Aggregation; Platelet Aggregation Inhibitors; Platelet Count; Platelet Function Tests; S-Nitrosoglutathione; S-Nitrosothiols; Thrombocytopenia; Tumor Necrosis Factor-alpha

2007
A point mutation leads to an unpaired cysteine residue and a molecular weight polymorphism of a functional platelet beta 3 integrin subunit. The Sra alloantigen system of GPIIIa.
    The Journal of biological chemistry, 1994, Mar-18, Volume: 269, Issue:11

    Topics: Amino Acid Sequence; Animals; Base Sequence; Blood Platelets; Cysteine; DNA; DNA Primers; Gene Frequency; Humans; Infant, Newborn; Molecular Sequence Data; Oligonucleotide Probes; Platelet Membrane Glycoproteins; Point Mutation; Polymorphism, Genetic; RNA, Messenger; Thrombocytopenia; Transfection

1994
A functional platelet fibrinogen receptor with a deletion in the cysteine-rich repeat region of the beta(3) integrin: the Oe(a) alloantigen in neonatal alloimmune thrombocytopenia.
    Blood, 2002, Feb-15, Volume: 99, Issue:4

    Topics: Adult; Antigens, CD; Antigens, Human Platelet; Cysteine; DNA Mutational Analysis; Female; Genetic Variation; Humans; Infant, Newborn; Integrin beta3; Isoantibodies; Isoantigens; Male; Maternal-Fetal Exchange; Pedigree; Platelet Glycoprotein GPIIb-IIIa Complex; Platelet Membrane Glycoproteins; Pregnancy; Pregnancy Complications, Hematologic; Repetitive Sequences, Amino Acid; Sequence Deletion; Thrombocytopenia

2002